Catalogue number 26920100, listed by Propper Manufacturing Co., Inc., United States, under Indicator, Biological Sterilization Process. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for BI-OK Steam Vials (100/pack) | Listed by | Propper Manufacturing Co., Inc., United States |
| FDA product code | FRC |
| Device type | Indicator, Biological Sterilization Process |
| Device class | Class 2 |
| Regulation | 21 CFR 880.2800 |
| 510(k) | K891784 |
| Record published | 2019-03-11 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Single use | Yes |
| Label carries | lot or batch number, expiry date |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.